coactiv+™ Antimicrobial Wound Gel

FDA 510(k) K223259 · Kane Biotech, Inc.

Substantially Equivalent

510(k) numberK223259

Submission

Device name
coactiv+™ Antimicrobial Wound Gel
Applicant
Kane Biotech, Inc.
Winnipeg, CA
Received
October 24, 2022
Decision date
May 24, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRO – Dressing, Wound, Drug
Device class
Unclassified

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K254041SkinSmart Antimicrobial HydroGelFRO · Traditional Magic Science Supply, LLC09/11/2026SE
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K253665Vashe Plus Antimicrobial SolutionFRO · Traditional Urgo Medical North America, LLC08/11/2026SE
K261023Microdacyn Wound Irrigation SolutionFRO · Traditional Sonoma Pharmaceuticals, Inc.06/24/2026SE
K251929SilverCeuticals® Antimicrobial Wound GelFRO · Traditional Silverceuticals, Inc.06/24/2026SE
K261638Bonvadis®FRO · Special Oneness Biotech Co., Ltd.06/17/2026SE
K254073StatSeal DiscFRO · Traditional Merit Medical Systems, Inc.05/13/2026SE
K254191IWD-Gel™FRO · Traditional InnovaCorium, Inc.04/07/2026SE
K252023MiraChlor Antimicrobial Wound SolutionFRO · Traditional Letus Corporation03/25/2026SE
K251999Promogran Prisma™ Collagen Matrix with ORC and SilverFRO · Traditional Solventum Germany GmbH03/13/2026SE

More from Solventum Germany GmbH

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K252759revyve® Antimicrobial Skin and Wound CleanserFRO · Traditional 01/08/2026SE
K241809coactiv+™ Antimicrobial Wound GelFRO · Special 07/19/2024SE

Questions and answers

When was coactiv+™ Antimicrobial Wound Gel cleared by the FDA?

coactiv+™ Antimicrobial Wound Gel (K223259) received a 510(k) decision of Substantially Equivalent on May 24, 2023, 212 days after the submission was received.

What is the product code of K223259?

The FDA product code is FRO – Dressing, Wound, Drug, a Unclassified device.